Initiation of low-flow anesthesia without wash-in following intubation
Initiation of low-flow anesthesia without wash-in following intubation: After endotracheal intubation, fresh gas flow is set to 0.75 L/min with 60% O₂. The sevoflurane vaporizer is initially set to 8%, and the sevoflurane concentration is subsequently titrated according to the target MAC value. Anesthesia depth and oxygenation are monitored using PSI monitoring and serial arterial blood gas measurements.
Study summary
This study aims to evaluate whether adjusting the fresh gas flow rate to low-flow immediately after intubation, without performing a wash-in, is a reliable approach with respect to depth of anesthesia and oxygenation.
Eligibility
Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* ASA physical status I-II
* Cases lasting longer than 30 minutes
* Non-laparoscopic surgical procedures
Exclusion Criteria:
* Patients with life-threatening renal, cardiac, or hepatic disease
* Patients with chronic pulmonary diseases such as asthma or COPD
* Patients with intraoperative hemodynamic instability
* Patients with a body mass index (BMI) lower than 20 or higher than 30
Primary outcome measure(s)
Comparison of arterial oxygen partial pressure (PaO₂) values between groups — Measured at 10, 20, 30, and 45 minutes after induction of anesthesia and before the end of surgery. Comparison of arterial oxygen partial pressure (PaO₂) and Patient State Index (PSI) values between groups.
Comparison of Patient State Index (PSI) values between groups. — Continuously monitored intraoperatively and recorded at 10, 20, 30, and 45 minutes after induction of anesthesia. PSI is an EEG-based index ranging from 0 to 100. Lower values indicate deeper anesthesia; the target range is 25-50 during general anesthesia.
Trial sites (1)
Facility
City
Region
Status
Binali Yildirim Univercity
Erzincan
Erzincan
More Erzincan Binali Yildirim Universitesi trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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